Author Archives: wames

Carers Week 8-14 June 2020: Making caring visible

Carers Week 2020: Making caring visible   Carers Week is an annual campaign to raise awareness of caring and highlight the challenges unpaid carers face recognise the contribution they make to families and communities throughout the UK help people who … Continue reading

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Impact of Coronavirus: people with chronic illness say “I feel forgotten”

Chronic Illness Inclusion Project blog post: “I feel forgotten”, by Anna Ruddock, June 1 2020   A submission to the Women and Equalities Committee about the impact of coronavirus on people with chronic illness. In April, the Women and Equalities … Continue reading

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Scientists call for more European research on ME/CFS

European ME Coalition Press Release: Scientists call for more European research on ME/CFS, 10 June 2020   More than one hundred scientists have signed an open letter calling for more European research into the illness Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS). … Continue reading

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Physical activity measures in patients with ME/CFS: correlations between peak oxygen consumption, the physical functioning scale of the SF-36 questionnaire, & the number of steps from an activity meter

Physical activity measures in patients with myalgic encephalomyelitis/chronic fatigue syndrome: correlations between peak oxygen consumption, the physical functioning scale of the SF-36 questionnaire, and the number of steps from an activity meter, by CMC van Campen, Peter C Rowe, Freek … Continue reading

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Health-related quality of life in Norwegian adolescents living with CFS

Health-related quality of life in Norwegian adolescents living with Chronic Fatigue Syndrome, by  Wenche Ann Similä, Vidar Halsteinli, Ingrid B Helland, Christer Suvatne, Hanna Elmi, Torstein Baade Rø in Health Qual Life Outcomes. 2020 Jun 5;18(1):170 [doi: 10.1186/s12955-020-01430-z]   Research … Continue reading

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The Health Minister, Covid-19, ME, rehabilitation & NICE

The Health Minister comments on Covid-19, ME, rehabilitation & NICE   The Health Minister Vaughan Gething has replied to the letter WAMES sent to him on International ME Awareness Day highlighting the links between Covid-19, PVFS and ME, and requesting … Continue reading

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The concept of ‘illness without disease’ impedes understanding of CFS: a response to Sharpe & Greco

The concept of ‘illness without disease’ impedes understanding of chronic fatigue syndrome: a response to Sharpe and Greco, by Steven Lubet, David Tuller in BMJ Medical Humanities. Published Online First: 01 June 2020. [doi: 10.1136/medhum-2019-011807]   Article abstract: In a … Continue reading

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Metabolic dysfunction in ME/CFS not due to anti-mitochondrial antibodies

Metabolic dysfunction in myalgic encephalomyelitis/chronic fatigue syndrome not due to anti-mitochondrial antibodies, by Isabell Nilsson, Jeremy Palmer, Eirini Apostolou, Carl-Gerhard Gottfries, Muhammad Rizwan, Charlotte Dahle and Anders Rosén in Front. Med., 31 March 2020 [doi.org/10.3389/fmed.2020.00108 ]   Research abstract: Metabolic profiling … Continue reading

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Modeling disability: softly making the invisible visible

Modeling disability: softly making the invisible visible, by Libby Evan (2020) Bachelor of Fine Arts Senior Papers 74   Research abstract: “I am not asking for pity. I am telling you about my disability.” – Eli Clare1 In the following … Continue reading

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Sleep problems in adolescents with CFS: a case-control study nested within a prospective clinical cohort

Sleep problems in adolescents with CFS: A case-control study nested within a prospective clinical cohort, by Maria Elizabeth Loades, Katharine A Rimes, Trudie Chalder in Clinical Child Psychology and Psychiatry, May 22 2020 [doi.org/10.1177/1359104520918364]   Research abstract: Sleep problems have … Continue reading

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